This is topic LLMD or LLND in MA or New England? in forum Seeking a Doctor at LymeNet Flash.


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Posted by dbpei (Member # 33574) on :
 
Wondering if anyone here can refer me to a good LLMD or LLND in central or western MA. I would also travel to nearby RI, NH, and CT for the right doctor. Would like to hear your experiences also. Thank you!
 
Posted by hopingandpraying (Member # 9256) on :
 
PM sent for CT & RI.
 
Posted by Jubbster (Member # 42919) on :
 
Hi,
I hope I am posting this correctly. I am in need of an LLMD in Massachusetts. I live about 30 mins directly North of Providence Rhode Island and about 30 mins south of Boston. The doctors here are not helping me Ive been in bed for 4 months sick with what I believe is Lymes. Igenex is testing now. I have had brain MRI's and Elisa tests all negative. Please help me if you have an LLMD. The Amox worked for 2 weeks and they wouldn't RX more.
Thank you so much
 
Posted by dbpei (Member # 33574) on :
 
PM being sent.
 
Posted by hopingandpraying (Member # 9256) on :
 
Jubbster - Welcome to Lymenet! PM sent for MA.

Sorry you are going through this. The ELISA test is very unreliable. Testing should be done through IGENEX Labs in Palo Alto, CA.

You need to be evaluated and treated by a LLMD. Non LLMDs have no clue about this horrible disease or its complex treatment.

You should write a new post instead of adding on to an existing one. That way, more people will see it and respond.

Also, please break up your posts into 2-3 sentence paragraphs ,as there are people on Lymenet who have neurological problems and cannot read large blocks of text. Thanks.

Check the online state Lyme groups at:
http://health.groups.yahoo.com/group/massachusettslyme

Some more resources for you:
www.lyme-aware.org/massachusetts.html

Read "Cure Unknown" by Pamela Weintraub. Check your local library or buy it used on Amazon.

View "Under Our Skin" for free on www.hulu.com
 
Posted by Nancy2 (Member # 95) on :
 
PM sent to Jubbster!
 


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